EP0697594B1 - Ion selective ceramic membrane - Google Patents

Ion selective ceramic membrane Download PDF

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Publication number
EP0697594B1
EP0697594B1 EP95109983A EP95109983A EP0697594B1 EP 0697594 B1 EP0697594 B1 EP 0697594B1 EP 95109983 A EP95109983 A EP 95109983A EP 95109983 A EP95109983 A EP 95109983A EP 0697594 B1 EP0697594 B1 EP 0697594B1
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EP
European Patent Office
Prior art keywords
ion selective
ceramic membrane
selective ceramic
doped
conductivity
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
EP95109983A
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German (de)
English (en)
French (fr)
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EP0697594A2 (en
EP0697594A3 (en
Inventor
Niels Christiansen
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Topsoe AS
Original Assignee
Haldor Topsoe AS
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Publication date
Application filed by Haldor Topsoe AS filed Critical Haldor Topsoe AS
Publication of EP0697594A2 publication Critical patent/EP0697594A2/en
Publication of EP0697594A3 publication Critical patent/EP0697594A3/en
Application granted granted Critical
Publication of EP0697594B1 publication Critical patent/EP0697594B1/en
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    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N27/00—Investigating or analysing materials by the use of electric, electrochemical, or magnetic means
    • G01N27/26—Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating electrochemical variables; by using electrolysis or electrophoresis
    • G01N27/28—Electrolytic cell components
    • G01N27/30—Electrodes, e.g. test electrodes; Half-cells
    • G01N27/333—Ion-selective electrodes or membranes

Definitions

  • the present invention relates to ion selective membranes and, in particular, to a proton conducting membrane of lanthanum phosphate ceramic material being able to operate in high temperature environment.
  • Ion selective membranes are key components in electrodes, whose electrical potentials are related to the activity of the ionic media, to which they are exposed.
  • Those membranes are conventionally composed of synthetic, polymeric organic ion exchange resins having high selectivity and low electrical resistance.
  • ion selective membranes composed of ceramic materials have also found applications in a wide variety of sensors.
  • the electrical properties of ceramic materials employed in sensors are effected by changes in temperature, atmosphere and in electrical parameters.
  • Ion conducting ceramics are presently conventionally employed in humidity-sensitive resistors, oxygen sensors and as electrolytes in fuel cells. Further applications utilize the proton conductivity of certain ceramic materials.
  • Known ceramics with proton conductivity include ceramics with perovskite structure, stannates and apatites.
  • probes for sensing hydrogen and steam comprising a sensor element including perovskite type proton conductive solid electrodes.
  • high temperature hydrogen sensors based on sintered metal oxide containing strontium, cerium, and zirconium are disclosed in Japanese Patent Application Nos. 59,125055 and 63,291868.
  • the disadvantage of the known proton conducting ceramic materials is changes of internal surfaces and disintegration during exposure of the materials to corrosive environment at high temperature.
  • the membranes must further have improved durability and reliability, when employed as sensor component in hydrogen activity monitoring devices.
  • this invention provides an ion selective ceramic membrane with high proton conductivity, which membrane is formed of a lanthanide phosphate with the monazite structure and being doped with one or more metals Me from Group IIA of the Periodic Table and having a composition: Ln 1-x Me x PO 4 wherein Ln is lanthanum, cerium, praseodymium, neodymium, samarium, europium and/or gadolinium; and 0 ⁇ x ⁇ 0.5.
  • Preparation of the ceramic material for use in the invention may be performed by conventional ceramic processing methods. Such methods include coprecipitation of lanthanum phosphate from aqueous solutions of soluble salts of lanthanum and an optional dopant, filtering of the precipitate and forming a membrane member by dry pressing, extrusion or injection moulding, succeeded by sintering in air at temperatures up to 1400°C.
  • the sintered lanthanide phosphate ceramic material is stable in atmospheric air and in corroding environment, like molten metals, and oxidizing or reducing atmospheres, at temperature up to 1300°C with a thermic expansion coefficient of about 9.8 ⁇ 10 -6 /°C.
  • the electrical conductivity of the material is proportional to the temperature and the proton activity in an ambient environment.
  • the conductivity of the material is partly attributed to native effects, like electron holes or oxygen vacancies, and partly to protons in the doped material through defects in the ceramic structure, where protons compensate for acceptor substituents in the presence of a hydrogen containing environment.
  • the material is, therefore, useful as sensor component for monitoring changes in relative humidity or hydrogen concentrations in different environments.
  • the conductivity of the material is further a function of the dopant metal and the temperature.
  • the conductivity of the doped material is further determined by the concentration of dopants in the material.
  • Doped materials with high conductivity and stability are obtained with the above dopants at concentrations of between 2 and 10 atom%.
  • Lanthanum phosphate samples doped with 5 atm% calcium or strontium were prepared by coprecipitation from 0.2 M aqueous solutions of (NH 4 ) 2 HPO 4 , La(NO 3 ) 3 ⁇ 6H 2 O and Sr(NO 3 ) 2 or Ca(NO 3 ) 2 .
  • the aqueous slurry obtained thereby was filtered, dried and calcined to a ceramic powder.
  • the powder was in a subsequent preparation step ball milled for 24 hours.
  • the powder was then cold-pressed at 1900 bar to a green body.
  • the green body was sintered in the presence of air at about 1200-1300°C.
  • the electrical conductivity of the sintered body was measured at temperatures up to 1100°C in dry and in wet air.
  • Fig. 1 shows proton conductivity of a membrane sample composed of Sr doped LaPO 4 having the composition La 0.95 Sr 0.05 PO 4 .
  • Conductivity was determined as a function of p(H 2 O) at 800°C. As seen from Fig. 1, conductivity increases as the vapour pressure increases in the atmosphere.
  • Fig. 2 represents results from measurements of conductivity obtained with the above doped lanthanum phosphate at different temperatures (1/T°K) in dry air ( ⁇ ) and in air with 2% H 2 O (O) within a temperature interval of between 600°C and 1200°C.

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  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Biochemistry (AREA)
  • General Physics & Mathematics (AREA)
  • Electrochemistry (AREA)
  • Physics & Mathematics (AREA)
  • Analytical Chemistry (AREA)
  • Molecular Biology (AREA)
  • General Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Immunology (AREA)
  • Pathology (AREA)
  • Conductive Materials (AREA)
  • Separation Using Semi-Permeable Membranes (AREA)
  • Investigating Or Analyzing Materials By The Use Of Fluid Adsorption Or Reactions (AREA)
  • Compositions Of Oxide Ceramics (AREA)
  • Fuel Cell (AREA)
EP95109983A 1994-08-17 1995-06-27 Ion selective ceramic membrane Expired - Lifetime EP0697594B1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
DK953/94 1994-08-17
DK095394A DK171537B1 (da) 1994-08-17 1994-08-17 Ionselektiv keramisk membran og anvendelse heraf
DK95394 1994-08-17

Publications (3)

Publication Number Publication Date
EP0697594A2 EP0697594A2 (en) 1996-02-21
EP0697594A3 EP0697594A3 (en) 1998-01-21
EP0697594B1 true EP0697594B1 (en) 2003-10-22

Family

ID=8099369

Family Applications (1)

Application Number Title Priority Date Filing Date
EP95109983A Expired - Lifetime EP0697594B1 (en) 1994-08-17 1995-06-27 Ion selective ceramic membrane

Country Status (10)

Country Link
US (1) US5632874A (ru)
EP (1) EP0697594B1 (ru)
JP (1) JP3471132B2 (ru)
AU (1) AU688069B2 (ru)
CA (1) CA2152651C (ru)
DE (1) DE69531979T2 (ru)
DK (1) DK171537B1 (ru)
NO (1) NO953222L (ru)
RU (1) RU2143944C1 (ru)
ZA (1) ZA956839B (ru)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2741339B1 (fr) * 1995-11-20 1997-12-12 Commissariat Energie Atomique Procede de fabrication de composes de type monazite dopes ou non en actinides et application au conditionnement des dechets radioactifs riches en actinides et en lanthanides
SE514689C2 (sv) 1998-06-12 2001-04-02 Bin Zhu Bränslecell
JP4542792B2 (ja) * 2004-01-26 2010-09-15 財団法人ファインセラミックスセンター 耐酸化材料及び非酸化物系複合材料
DE102004014136B4 (de) * 2004-03-23 2007-12-06 Siemens Ag Anordnung mit einer Batterie
US7641997B2 (en) * 2004-09-23 2010-01-05 Ut-Battelle Llc Design and synthesis of guest-host nanostructures to enhance ionic conductivity across nanocomposite membranes
US7625653B2 (en) * 2005-03-15 2009-12-01 Panasonic Corporation Ionic conductor

Family Cites Families (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3727058A (en) * 1971-02-16 1973-04-10 Hughes Aircraft Co Hydrogen ion device
US4179491A (en) * 1976-11-15 1979-12-18 National Research Development Corporation Electrical device with separator as conductor for hydrogen cations
JPS5912055A (ja) * 1982-07-12 1984-01-21 株式会社日立製作所 交流エレベ−タ−の速度制御装置
JPS59125055A (ja) 1983-01-05 1984-07-19 Toyo Soda Mfg Co Ltd 高温水素センサ−
US4689122A (en) * 1983-12-29 1987-08-25 Uop Inc. Gas detection apparatus and method with novel electrolyte membrane
US4664757A (en) * 1985-12-27 1987-05-12 Uop Inc. Method and apparatus for gas detection using proton-conducting polymers
JP2616772B2 (ja) 1987-05-22 1997-06-04 株式会社デンソー プロトン導電性セラミックスの製造方法
JPH0756478B2 (ja) * 1990-03-27 1995-06-14 東京窯業株式会社 挿入式センサプローブ
DD294346A5 (de) * 1990-05-11 1991-09-26 Junkalor Gmbh Dessau,De Alkaliionenleitender festelektrolyt fuer gassensoren
US5213911A (en) * 1991-10-17 1993-05-25 The United States Of America As Represented By The United States Department Of Energy Solid-oxide fuel cell electrolyte
KR970003280B1 (ko) 1991-11-26 1997-03-17 도오교오 요오교오 가부시끼가이샤 용융금속중의 수소용해량 측정용 센서 프로우브 및 수소농도 측정방법
US5393404A (en) * 1993-06-17 1995-02-28 Rutgers, The State University Of New Jersey Humidity sensor with nasicon-based proton-conducting electrolyte

Also Published As

Publication number Publication date
DE69531979D1 (de) 2003-11-27
AU2854995A (en) 1996-02-29
EP0697594A2 (en) 1996-02-21
JPH08206476A (ja) 1996-08-13
ZA956839B (en) 1996-03-28
RU2143944C1 (ru) 2000-01-10
DK171537B1 (da) 1996-12-23
JP3471132B2 (ja) 2003-11-25
DK95394A (da) 1996-02-18
AU688069B2 (en) 1998-03-05
NO953222D0 (no) 1995-08-16
CA2152651C (en) 2001-02-20
US5632874A (en) 1997-05-27
NO953222L (no) 1996-02-19
CA2152651A1 (en) 1996-02-18
EP0697594A3 (en) 1998-01-21
DE69531979T2 (de) 2004-08-12

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